En-tête de navigationNavigation principaleSuiviFiche


Unité de recherche
PCRD EU
Numéro de projet
95.0865
Titre du projet
Controlled ripening and increased storage life of fruit and vegetables through ethylene control
Titre du projet anglais
Controlled ripening and increased storage life of fruit and vegetables through ethylene control

Textes relatifs à ce projet

 AllemandFrançaisItalienAnglais
Mots-clé
-
-
-
Anzeigen
Autre Numéro de projet
-
-
-
Anzeigen
Programme de recherche
-
-
-
Anzeigen
Description succincte
-
-
-
Anzeigen
Partenaires et organisations internationales
-
-
-
Anzeigen
Résumé des résultats (Abstract)
-
-
-
Anzeigen
Références bases de données
-
-
-
Anzeigen

Textes saisis


CatégorieTexte
Mots-clé
(Anglais)
ethylene; biotechnology; fruit ripening; vegetables; signal transduction
Autre Numéro de projet
(Anglais)
EU project number: FAIR-CT95-0225
Programme de recherche
(Anglais)
EU-programme: 4. Frame Research Programme - 4.3 Biomedical/Health research
Description succincte
(Anglais)
See abstract
Partenaires et organisations internationales
(Anglais)
Profs. Woltering, Pech, Grierson, Kanellis, Dortoglu, Hosemans, Tardieu, Papamethakis

Coordinator: Dienst Landbouwkundig Ouderzoek (NL)
Résumé des résultats (Abstract)
(Anglais)
Plant cells respond with increased production of the stress hormone ethylene when treated with elicitor preparations. The response involves a rapid increase in activity of 1-aminocyclopropane-1-carboxylic acid (ACC) synthase, the enzyme catalyzing the first step of ethylene biosynthesis. In some cases, the induction of this enzyme activity occurs at the posttranscriptional level and can be interrupted by removal of the elicitor or by the addition of protein kinase inhibitors.
To elucidate factors involved in elicitor-induced posttranscriptional ACC synthase (ACS) regulation, particularly its stability and a possible role of the ubiquitin/proteasome pathway we transformed suspension cultured plant cells with a cDNA encoding ACS under the control of a strong constitutive promoter. The transformed cell lines produced increased amounts of ACC and ethylene, but were strongly selected against overexpression of the transgene. Therefore, our future work will involve the use of an inducible promoter. Similar studies were conducted in Saccharomyces cerevisiae, using an inducible promoter system to heterologously express ACC synthase in wild type and mutant strains with a defective proteasome. The proteasome mutations did not affect the stability of ACS in this system. Moreover, elicited plant cells were treated with the highly efficient proteasome inhibitor MG132. These plant cells showed a strong increase of ACS activity, suggesting a possible role of the proteasome in the regulation of ACC synthase and the production of ethylene.

Références bases de données
(Anglais)
Swiss Database: Euro-DB of the
State Secretariat for Education and Research
Hallwylstrasse 4
CH-3003 Berne, Switzerland
Tel. +41 31 322 74 82
Swiss Project-Number: 95.0865